A Parental Educational Intervention to Facilitate Informed Consent for Pediatric Procedural Sedation in the Emergency Department

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01850329

Enrollment

Registered

2013-05-09

Start date

2009-12-07

Completion date

2014-09-09

Last updated

2017-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Informed Consent Process

Brief summary

This study is planning to develop the computed-assisted information program and determine whether the computed-assisted information program are superior to routine discussion for informing parents in the emergency department (ED) about risks, benefits, and alternatives to receiving procedural sedation for their children.

Interventions

OTHERcomputed-assisted information program

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

No minimum to 18 Years

Healthy volunteers

Inclusion criteria

* Parents with patients under 18 years of age * patients receive the procedural sedation and anesthesia in the emergency department

Exclusion criteria

* clinically unstable * refuse to participate * unable to understand the consent process for this study

Design outcomes

Primary

Measure	Time frame	Description
structured questionnaire	before and immediately after the intervention when participants are in the emergency department, it is expected to take an expected average time of one hour	a structured questionnaire with knowledge measure and satisfaction will be delivered to the participants for data collection.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026